A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv6056n54



Internal ID22773951
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:70284647..70287994hg38UCSC Ensembl
chr18:67951883..67955230hg19UCSC Ensembl
chr18:66102863..66106210hg18UCSC Ensembl
Cytoband18q22.2
Allele length
AssemblyAllele length
hg383348
hg193348
hg183348
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv577551, nsv577549, nsv577550, nsv577548
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv6056n54
Frequency
Sample Size17421
Observed Gain0
Observed Loss15
Observed Complex0
Frequencyn/a


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